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. 2020 Aug 3;11(3):748–787. doi: 10.1007/s13346-020-00818-0

Table 6.

Hybrid nanoformulation

Diseases Antiviral drug Type of nanodelivery system Lipid and polymer which used as carrier Problems encountered Key findings Ref
HIV/AIDS Zidovudine Lipid–polymer hybrid nanoparticles

Stearic acid, Compritol 888 ATO, polymer

Gelatin

Low aqueous solubility

Short half-life and high side effects

High loading, hemocompatibility, sustained release [232]
HIV/AIDS Zidovudine Lipid–polymer hybrid nanoparticles Alginate, stearic acid, PEG Biocompatibility problems, high toxicity Biocompatibility, superior drug-loading capacity, and enhanced drug release efficacy [233]
HIV/AIDS Nevirapine Lipid–polymer hybrid nanoparticles PEG 400, propylene glycol, polyoxyethylene polyoxypropylene (copolymer), glyceryl monostearate, polyglyceryl distearate Decreased solubility Increased drug delivery to target sites [233]
HIV/AIDS Zidovudine Core shell nanoparticle Long-chain fatty acid, stearic acid, PEG, dextran Biodegradability and biocompatibility High stability, controlled drug release [234]
HIV/AIDS Zidovudine Core shell nanoparticle PVP, stearic acid, PEG

Short half-life

Low bioavailability

Decreased systemic side effects, useful therapeutic activity [235]